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1.
J Pediatr ; 173: 149-53, 2016 06.
Article in English | MEDLINE | ID: mdl-26979650

ABSTRACT

OBJECTIVES: To determine the clinical course of adolescent-onset postural orthostatic tachycardia syndrome (POTS) and to assess health-related quality of life, 2-10 years after diagnosis. STUDY DESIGN: Pediatric patients, 13-18 years of age, diagnosed with POTS at Mayo Clinic, Rochester, from 2003 to 2010 were mailed a questionnaire if they were at least 18 years of age at the time of the mailing. The primary outcome measures were norm-based, age- and sex-adjusted, 36-Item Short Form Health Survey physical composite score and mental composite score. RESULTS: The survey was mailed to 502 patients with a response rate of 34% (n = 172). The mean duration from diagnosis to survey completion was 5.4 (SD, 1.9) years; the mean age of the respondents at the time of the survey was 21.8 (2.2) years. The responders were predominantly females (84% vs 68% of nonresponders; P < .001). Only 33 (19%) respondents reported complete resolution of symptoms, and an additional 51% reported persistent but improved symptoms, and 28 (16%) had only intermittent symptoms. The majority (71%) consider their health at least "good." The mean physical composite score was significantly lower than the population norm (mean [SD], 36.6 [15.8] vs 50; P < .001), however, the corresponding mean mental composite score was normal (50.1 [11.2]). CONCLUSIONS: Overall, 86% of adolescents with POTS report resolved, improved, or just intermittent symptoms, when assessed via questionnaire at an average of 5 years after initial treatment. Patients with persistent symptoms have more physical than mental health concerns.


Subject(s)
Health Status , Postural Orthostatic Tachycardia Syndrome/physiopathology , Quality of Life , Adolescent , Female , Follow-Up Studies , Humans , Male , Mental Health , Postural Orthostatic Tachycardia Syndrome/therapy , Recurrence , Remission, Spontaneous , Severity of Illness Index , Surveys and Questionnaires , Young Adult
2.
Int J Pediatr Otorhinolaryngol ; 113: 119-123, 2018 Oct.
Article in English | MEDLINE | ID: mdl-30173969

ABSTRACT

OBJECTIVE: This study sought to evaluate the impact of an interdisciplinary care model for pediatric aerodigestive patients in terms of efficiency, risk exposure, and cost. METHODS: Patients meeting a standard clinical inclusion definition were studied before and after implementation of the aerodigestive program. RESULTS: Aerodigestive patients seen in the interdisciplinary clinic structure achieved a reduction in time to diagnosis (6 vs 150 days) with fewer required specialist consultations (5 vs 11) as compared to those seen in the same institution prior. Post-implementation patients also experienced a significant reduction in risk, with fewer radiation exposures (2 vs 4) and fewer anesthetic episodes (1 vs 2). Total cost associated with the diagnostic evaluation was significantly reduced from a median of $10,374 to $6055. CONCLUSION: This is the first study to utilize a pre-post cohort to evaluate the reduction in diagnostic time, risk exposure, and cost attributable to the reorganization of existing resources into an interdisciplinary care model. This suggests that such a model yields improvements in care quality and value for aerodigestive patients, and likely for other pediatric patients with chronic complex conditions.


Subject(s)
Gastrointestinal Diseases/diagnosis , Gastrointestinal Diseases/therapy , Patient Care Team/organization & administration , Respiratory Tract Diseases/diagnosis , Respiratory Tract Diseases/therapy , Child , Child, Preschool , Efficiency, Organizational , Female , Gastrointestinal Diseases/economics , Humans , Infant , Male , Models, Organizational , Respiratory Tract Diseases/economics , Retrospective Studies
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